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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516756Generated: November 4, 2026

Hydrochloric Acid → Ethyl 2-(3-chloro-4-nitrophenyl)propanoate

https://huagongshe.com/reaction/1516756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Chloro-2-nitrobenzeneHCID 6945—
ReactantEthyl 2-chloropropionateHCID 10807—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-(3-chloro-4-nitrophenyl)propanoateHCID 1321376764%

Reaction Conditions

Temperature0 °C

Reaction Steps

Potassium tert-butylate (11.22 g, 2 eq) is added to a solution of DMF (80 ml) cooled down to 0° C. A solution of 1-chloro-2-nitrobenzene (7.87 g, 1 eq) and ethyl 2-chloropropanoate (7 ml, 1.1 eq) is added dropwise over 45 minutes to the mixture keeping the reaction temperature below 5° C. At the end of the addition, stirring is maintained for 2 hours at 0° C. then the mixture is hydrolyzed at this temperature by a 1N hydrochloric acid solution and ethyl acetate is added. After decantation and extractions, the combined organic phases are washed with salt water, dried over Na2SO4 and concentrated under reduced pressure. Purification by flash chromatography on silica gel (eluent: heptane/dichloromethane 8:2 to 6:4) produces the expected compound in the form of a yellow oil (8.28 g; 64% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08227485B2
Source datasetuspto-grants-2012_07
ORD IDord-06ed9330c31e41d39a1393b14ccbcf10
Source noteuspto-grants-2012_07